Journal article
Authors list: Becker, K; Christopherson, RJ; Cowden, WB; Hunt, HN; Schirmer, RH
Publication year: 1990
Pages: 59-65
Journal: Biochemical Pharmacology
Volume number: 39
Issue number: 1
ISSN: 0006-2952
DOI Link: https://doi.org/10.1016/0006-2952(90)90648-5
Publisher: Elsevier
10-(4′-Chlorophenyl)-3-methylflavin has antimalarial activity in vitro and in vivo (Cowden et al., J Med Chem31:
Abstract:
799, 1988). This flavin analog and two of its derivatives were found to
inhibit the antioxidant flavoenzyme glutathione reductase from human
erythrocytes in its isolated form as well as in hemolysates. The
mixed-type inhibition was completely reversible, the Ki-values
being of the order of 1 μM. Surprisingly, the drugs were not
competitive with FAD, but with GSSG, one of the enzyme's substrates.
Malaria parasite glutathione reductase, extracted from Plasmodium falciparum, could also be inhibited by the compounds. Studies on the effects of the substances on P. falciparum in vitro,
which were demonstrated morphologically and by growth inhibition,
confirmed previous observations with 10-(4′-chlorophenyl)-3-methylflavin
and showed similar parasiticidal characteristics for the two new
derivatives. The activities of five other erythrocytic enzymes tested
were not impaired by the drugs, nor was the nucleotide metabolism of
erythrocytes and/or parasites significantly changed. Permeation into red
blood cells was demonstrated for one compound by 19F-NMR-spectroscopy.
Inhibition of glutathione reductase might contribute to, or account
for, the antimalarial activity of this group of flavin analogs.
Citation Styles
Harvard Citation style: Becker, K., Christopherson, R., Cowden, W., Hunt, H. and Schirmer, R. (1990) Flavin analogs with antimalarial activity as glutathione reductase inhibitors, Biochemical Pharmacology, 39(1), pp. 59-65. https://doi.org/10.1016/0006-2952(90)90648-5
APA Citation style: Becker, K., Christopherson, R., Cowden, W., Hunt, H., & Schirmer, R. (1990). Flavin analogs with antimalarial activity as glutathione reductase inhibitors. Biochemical Pharmacology. 39(1), 59-65. https://doi.org/10.1016/0006-2952(90)90648-5